US4386009A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Method and system for ethanol production
Assignee: United States Department of Energy
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Filing: 1981-09-24
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Granted: 1983-05-31
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Expires: 2001-09-24
Abstract
Abstract A transition metal carbonyl and a tertiary amine are employed as a homogeneous catalytic system in methanol or a less volatile solvent to react methanol with carbon monoxide and hydrogen gas producing ethanol and carbon dioxide. The gas contains a high carbon monoxide to hydrogen ratio as is present in a typical gasifier product. The reaction has potential for anhydrous ethanol production as carbon dioxide rather than water is produced. Selected transition metal carbonyls include those of iron, rhodium ruthenium, manganese in combination with iron and possibly osmium. Selected amines include trimethylamine, N-Methylpyrrolidine, 2,4-diazabicyclooctane, dimethylneopentylamine, N-methylpiperidine and derivatives of N-methylpiperidine.
Inventors
- 👤 Harold M. Feder
- 👤 Michael J. Chen
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 06:57
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/16; B01J31/20; B01J31/02; B01J31/0234; B01J31/0235; B01J31/0237; C; C07; C07C; C07C29/00; C07C29/32; B01J2231/00; B01J2231/30; B01J2231/34; B01J2231/60; B01J2231/64; B01J2231/641; B01J2531/00; B01J2531/70; B01J2531/72; B01J2531/80; B01J2531/82; B01J2531/821; B01J2531/822; B01J2531/825; B01J2531/84; B01J2531/842
Claims Analysis
Total Claims: 17
Claim 1
Independent Claim
68 words
A homogeneous catalytic system in organic solution for the conversion of methanol to ethanol in accordance with the reaction MeOH+2CO+H 2 →EtOH+CO 2 comprising: organic solvent including methanol; a tertiary amine in the organic solution; and a combination of transition metal carbonyl species in the organic solution selected from the group consisting of iron carbonyl species with manganese carbonyl species and iron carbonyl species with rhodium carbonyl species.
Claim 2
Dependent Claim
68 words
A homogeneous catalytic system in organic solution for the conversion of methanol to ethanol in accordance with the reaction MeOH+2CO+H 2 →EtOH+CO 2 comprising: organic solvent including methanol; a tertiary amine in the organic solution; and a combination of transition metal carbonyl species in the organic solution selected from the group consisting of iron carbonyl species with manganese carbonyl species and iron carbonyl species with rhodium carbonyl species.
Claim 3
Dependent Claim
23 words
The catalytic system of claim 1 wherein a mixture of iron carbonyl species and manganese carbonyl species are present in the organic solution.
Claim 4
Dependent Claim
39 words
The catalytic system of claim 2 wherein the iron of the iron carbonyl species is present in the organic solution in a mole ratio of about 1:1 to 5:1 with respect to the manganese of the manganese carbonyl species.
Claim 5
Dependent Claim
38 words
The catalytic system of claim 2 wherein said iron carbonyl species include those provided by blending Fe(CO) 5 into the solution and said manganese carbonyl species include those provided by blending Mn 2 (CO) 10 into the solution.
Claim 6
Dependent Claim
34 words
The catalytic system of claim 4 wherein the solution includes the combination of the species HFe(CO) 4 - , Fe(CO) 4 -2 Mn 2 (CO) 10 , Mn(CO) 5 - and HMn(CO) 5 .
Claim 7
Dependent Claim
18 words
The catalytic system of claim 1 wherein carbon monoxide and hydrogen gas are dissolved in the organic solvent.
Claim 8
Dependent Claim
19 words
The catalytic system of claim 6 wherein sufficient carbon monoxide and hydrogen are present to maintain methylformate in solution.
Claim 9
Dependent Claim
18 words
The catalytic system of claim 1 wherein said tertiary amine is an acyclic, alicyclic or a heterocyclic amine.
Claim 10
Dependent Claim
56 words
The catalytic system of claim 8 wherein said tertiary amine is selected from the group of acyclic, alicyclic and heterocyclic amines consisting of N-methylpiperidine, heterocyclic amines including N-methylpiperidine substituents on an acyclic chain, heterocyclic amines including alkyl substituents on an N-methylpiperidine ring or on an N-methylpiperidyl substituent ring, trimethylamine, N-methylpyrrolidine, 1,4-diazabicyclooctane and 1,8 bis (dimethylamino) naphthalene.
Claim 11
Dependent Claim
43 words
The catalytic system of claim 9 wherein said tertiary amine is selected from the group of heterocyclic amines consisting of N-methylpiperidine, amines including N-methylpiperidyl substituents on an alkane and amines with alkyl substituents on an N-methylpiperidine ring or on an N-methylpiperidyl substituent ring.
Claim 12
Dependent Claim
23 words
The system of claim 10 wherein said tertiary amine is selected from the group of heterocyclic amines consisting of N-methylpiperidine and 1,3-di (1-methyl-4-piperidyl)propane.
Claim 13
Dependent Claim
38 words
The catalytic system of claim 1 wherein the transition metal carbonyl species, the tertiary amine and a protonated tertiary amine species are each present in the solution in reactable quantities in excess of 10 -5 moles per liter.
Claim 14
Dependent Claim
27 words
The catalytic system of claim 1 wherein the measured effective pH of the solution is between 9-13 and the solution includes less than 4 weight percent water.
Claim 15
Dependent Claim
44 words
The catalytic system of claim 1 wherein the organic solvent includes methanol and an organic co-solvent selected from the group of organic liquids consisting of dimethylether of diethylene glycol (diglyme), ethoxyethanol, tetraglyme butanol, saturated alcohols of four or more carbons, glycols, 1-methylpyrrolidinone-2 and tetrahydrothiophene-1,1-dioxide.
Claim 16
Dependent Claim
21 words
The catalytic system of claim 14 wherein said co-solvent comprises 1-methylpyrrolidinone-2 to extend the life of the transition metal carbonyl catalyst.
Claim 17
Dependent Claim
31 words
The catalytic system of claim 1 wherein a combination of iron and manganese carbonyl species along with 1,3 di(N-methyl-4-piperidyl)propane are present in a solvent of methanol and a co-solvent of N-methylpyrrolidine-2.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1986-05-30 | 1986-11-29 | 1987-05-31 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1990-05-30 | 1990-11-29 | 1991-05-31 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1994-05-30 | 1994-11-29 | 1995-05-31 | $7700.00 | Window Closed / Lapsed |